| Título : |
TPEN selectively eliminates lymphoblastic B cells from bone marrow pediatric acute lymphoblastic leukemia patients |
| Tipo de documento : |
documento electrónico |
| Autores : |
Lina María Quiroz Duque, ; Alexandra Restrepo Rincón, ; Natalia Andrea Valencia Zuluaga, |
| Fecha de publicación : |
2022 |
| Títulos uniformes : |
BioMetals
|
| Idioma : |
Inglés (eng) |
| Palabras clave : |
Acute leukemia Caspase-3 Chemoresistant DJ-1 PUMA Reactive oxygen species Signaling TP53 TPEN |
| Resumen : |
B-cell acute lymphoblastic leukemia (B-ALL) is a hematologic disorder characterized by the abnormal proliferation and accumulation of immature B-lymphoblasts arrested at various stages of differentiation. Despite advances in treatment, a significant percentage of pediatric patients with precursor B-ALL still relapse. Therefore, alternative therapies are needed to improve the cure rates for pediatric patients. TPEN (N, N, N’, N’-tetrakis(2-pyridylmethyl)-ethylenediamine) is a pro-oxidant agent capable of selectively inducing apoptosis in leukemia cell lines. Consequently, it has been suggested that TPEN could be a potential agent for oxidative therapy. However, it is not yet known whether TPEN can selectively destroy leukemia cells in a more disease-like model, for example, the bloodstream and bone marrow (BM), ex vivo. This investigation is an extension of a previous study that dealt with the effect of TPEN on ex vivo isolated/purified refractory B-ALL cells. Here, we evaluated the effect of TPEN on whole BM from nonleukemic patients (control) or pediatric patients diagnosed with de novo B-ALL or refractory B-ALL cells by analyzing the hematopoietic cell lineage marker CD34/CD19. Although TPEN was innocuous to nonleukemic BM (n = 3), we found that TPEN significantly induced apoptosis in de novo (n = 5) and refractory B-ALL (n = 6) leukemic cell populations. Moreover, TPEN significantly increased the counts of cells positive for the oxidation of the stress sensor protein DJ-1, a sign of the formation of H2O2, and significantly increased the counts of cells positive for the pro-apoptotic proteins TP53, PUMA, and CASPASE-3 (CASP-3), indicative of apoptosis, in B-ALL cells. We demonstrate that TPEN selectively eliminates B-ALL cells (CD34 + /CD19 +) but no other cell populations in BM (CD34 + /CD19-; CD34-/CD19 + ; CD34-/CD19-) independent of age, diagnosis status (de novo or refractory), sex, karyotype, or immunophenotype. Understanding TPEN-induced cell death in leukemia cells provides insight into more effective therapeutic oxidation-inducing anticancer agents. |
| Mención de responsabilidad : |
M. Mendivil-Perez, C. Velez-Pardo, L. M. Quiroz-Duque, A. Restrepo-Rincon, N. A. Valencia-Zuluaga & Marlene Jimenez-Del-Rio |
| Referencia : |
Biometals. 2022 Aug;35(4):741-758. |
| DOI (Digital Object Identifier) : |
10.1007/s10534-022-00397-2 |
| PMID : |
35635647 |
| En línea : |
https://link.springer.com/article/10.1007/s10534-022-00397-2 |
| Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=6030 |
TPEN selectively eliminates lymphoblastic B cells from bone marrow pediatric acute lymphoblastic leukemia patients [documento electrónico] / Lina María Quiroz Duque, ; Alexandra Restrepo Rincón, ; Natalia Andrea Valencia Zuluaga, . - 2022. Obra : BioMetalsIdioma : Inglés ( eng) | Palabras clave : |
Acute leukemia Caspase-3 Chemoresistant DJ-1 PUMA Reactive oxygen species Signaling TP53 TPEN |
| Resumen : |
B-cell acute lymphoblastic leukemia (B-ALL) is a hematologic disorder characterized by the abnormal proliferation and accumulation of immature B-lymphoblasts arrested at various stages of differentiation. Despite advances in treatment, a significant percentage of pediatric patients with precursor B-ALL still relapse. Therefore, alternative therapies are needed to improve the cure rates for pediatric patients. TPEN (N, N, N’, N’-tetrakis(2-pyridylmethyl)-ethylenediamine) is a pro-oxidant agent capable of selectively inducing apoptosis in leukemia cell lines. Consequently, it has been suggested that TPEN could be a potential agent for oxidative therapy. However, it is not yet known whether TPEN can selectively destroy leukemia cells in a more disease-like model, for example, the bloodstream and bone marrow (BM), ex vivo. This investigation is an extension of a previous study that dealt with the effect of TPEN on ex vivo isolated/purified refractory B-ALL cells. Here, we evaluated the effect of TPEN on whole BM from nonleukemic patients (control) or pediatric patients diagnosed with de novo B-ALL or refractory B-ALL cells by analyzing the hematopoietic cell lineage marker CD34/CD19. Although TPEN was innocuous to nonleukemic BM (n = 3), we found that TPEN significantly induced apoptosis in de novo (n = 5) and refractory B-ALL (n = 6) leukemic cell populations. Moreover, TPEN significantly increased the counts of cells positive for the oxidation of the stress sensor protein DJ-1, a sign of the formation of H2O2, and significantly increased the counts of cells positive for the pro-apoptotic proteins TP53, PUMA, and CASPASE-3 (CASP-3), indicative of apoptosis, in B-ALL cells. We demonstrate that TPEN selectively eliminates B-ALL cells (CD34 + /CD19 +) but no other cell populations in BM (CD34 + /CD19-; CD34-/CD19 + ; CD34-/CD19-) independent of age, diagnosis status (de novo or refractory), sex, karyotype, or immunophenotype. Understanding TPEN-induced cell death in leukemia cells provides insight into more effective therapeutic oxidation-inducing anticancer agents. |
| Mención de responsabilidad : |
M. Mendivil-Perez, C. Velez-Pardo, L. M. Quiroz-Duque, A. Restrepo-Rincon, N. A. Valencia-Zuluaga & Marlene Jimenez-Del-Rio |
| Referencia : |
Biometals. 2022 Aug;35(4):741-758. |
| DOI (Digital Object Identifier) : |
10.1007/s10534-022-00397-2 |
| PMID : |
35635647 |
| En línea : |
https://link.springer.com/article/10.1007/s10534-022-00397-2 |
| Enlace permanente : |
https://hospitalpablotobon.cloudbiteca.com/pmb/opac_css/index.php?lvl=notice_display&id=6030 |
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